FDA Inspection 749662 — ActiTech, LP
The FDA completed an inspection of ActiTech, LP on Aug 23, 2011 in Sherman, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Aug 23, 2011
- Fiscal Year
- 2011
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Sherman, TX (United States)